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The Rehabilitation of Atrophic Jaws Using Short Implants With Different Surface Characteristics

Not Applicable
Completed
Conditions
Periimplantitis
Osseointegration Failure of Dental Implant
Peri-Implantation Loss
Periodontal Bone Loss
Gingival Inflammation
Implant Complication
Interventions
Device: implants placement
Registration Number
NCT05766878
Lead Sponsor
University of Foggia
Brief Summary

The aim of the research is to evaluate the clinical outcome of short dental implants, characterized by a new macro-structural design and inserted in the upper or lower jaw in patients with reduced bone volume. The clinical outcomes will be compared for different surface treatments of implant neck and those of prosthetic components.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
30
Inclusion Criteria
  • healthy patients, with edentulous maxillary or mandibular ridge, requiring rehabilitation with two adjacent implants;
  • at least 6 month after extraction;
Exclusion Criteria
  • post-extractive implants;
  • sites requiring bone regeneration or maxillary sinus lift;
  • general health problems that contraindicate implant treatment.

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
machined collarimplants placementThe arm will be constituted by healthy people, that need to be rehabilitated by dental implant placement. A short implant (length 6mm; diameter 4.3) will be inserted in an edentulous site. The implant will present a surface treated with double acid etching and traditional machined collar. A definitive transgingival standard machined abutment will be immediately screwed. Four months later, prosthetic procedures will start.
anodized collarimplants placementThe arm will be constituted by healthy people, that need to be rehabilitated by dental implant placement. A short implant (length 6mm; diameter 4.3) will be inserted in an edentulous site. The implant will present a surface treated with double acid etching and anodized collar. A definitive transgingival anodized abutment will be immediately screwed. Four months later, prosthetic procedures will start.
Primary Outcome Measures
NameTimeMethod
Marginal Bone remodeling around the implant0-4-12 months after implant placement

The marginal bone remodeling will be evaluated by Radiographic examination. Periapical radiographs will be performed using paralleling technique with a Rinn-type positioner, customized for each patient at implant placement (T0), prosthetic restoration delivery (T1), and after 12 months (T2).Peri-implant bone levels will be measured at each time point as the linear distance (in mm) between implant platform and bone crest at mesial and distal aspects of each implant. A positive value will be assigned if the bone crest is coronal to the implant platform, whereas a negative value will be assigned if the first bone-to implant contact is apical to the implant platform. All measurements will be performed by two examiners, using measuring software (Image J). Each measurement will be performed three times at three different points.

Secondary Outcome Measures
NameTimeMethod
Periodontal indexes: Probing DepthThe measurements will be performed at 4 (T1) and 12 (T2) months after implant placement.

Probing Depth (PD) will be calculated as the distance (in mm) from the gingival peri-implant margin to the bottom of the peri-implant pocket.

Implant Stability evaluation0-4 months.

Primary and secondary implant stability will be measured with resonance frequency analysis (RFA) and subsequently expressed as an implant stability quotient (ISQ). The Implant stability will be measured immediately after placement (T0) and at 4 months (T1) after placement, when the osseointegration is supposed to take place.

Suppuration on probingThe measurements will be performed at 4 (T1) and 12 (T2) months after implant placement.

Suppuration on probing (SUP) will be scored dichotomously (Yes/No). The probing will be performed on 6 sites around the implant (3 buccal and 3 palatal/lingual) and appearance of pus or purulent exudate will be registered (Yes). The final score will be expressed as number of suppurative sites/total of probed sites (%)

Bleeding on ProbingThe measurements will be performed at 4 (T1) and 12 (T2) months after implant placement.

Bleeding on probing (BoP) will be scored dichotomously (Yes/No). The probing will be performed on 6 sites around the implant (3 buccal and 3 palatal/lingual) and appearance of blood will be registered (Yes). The final score will be expressed as number of bleeding sites/total of probed sites (%)

Plaque index of peri-implant tissuesThe measurements will be performed at 4 (T1) and 12 (T2) months after implant placement.

Plaque Index (PI) will be calculated by assigning a binary score to each surface (1= plaque present, 0 = plaque absent).

Trial Locations

Locations (3)

Clinica Odontoiatrica, University of Foggia

🇮🇹

Foggia, Italy

University of Genoa

🇮🇹

Genova, Italy

University of Turin

🇮🇹

Torino, Italy

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